510(k) K912760

AD-TECH EPIDURAL PEG ELECTRODE by Ad-Tech Medical Instrument Corp — Product Code GYC

K912760 is an FDA 510(k) premarket notification submitted by Ad-Tech Medical Instrument Corp for the device "AD-TECH EPIDURAL PEG ELECTRODE". The FDA issued a decision of Substantially Equivalent on January 15, 1992. The device falls under product code GYC (Electrode, Cortical), a Class II device regulated under 21 CFR 882.1310. Ad-Tech Medical Instrument Corp has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 15, 1992
Date Received
June 24, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Electrode, Cortical
Device Class
Class II
Regulation Number
882.1310
Review Panel
NE
Submission Type